Basic information Uses Safety Supplier Related

6-METHOXY-PYRIDINE-2-CARBOXYLICACIDMETHYLESTER

Basic information Uses Safety Supplier Related

6-METHOXY-PYRIDINE-2-CARBOXYLICACIDMETHYLESTER Basic information

Product Name:
6-METHOXY-PYRIDINE-2-CARBOXYLICACIDMETHYLESTER
Synonyms:
  • Methyl 6-methoxypicolinate
  • 2-Pyridinecarboxylic acid, 6-Methoxy-, Methyl ester
  • 6-Methoxy-2-Pyridinecarboxylic Acid Methyl Ester
  • methyl 6-methoxy-2-pyridinecarboxylate
  • Methyl 6-methoxy
  • 6-Methoxypyridinecarboxylic acid methyl ester
  • Methyl 6-methoxypyridine-2-carboxylate
CAS:
26256-72-4
MF:
C8H9NO3
MW:
167.16
Product Categories:
  • Building Blocks
  • C8 to C9
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Pyridines
Mol File:
26256-72-4.mol
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6-METHOXY-PYRIDINE-2-CARBOXYLICACIDMETHYLESTER Chemical Properties

Melting point:
33-38℃
Boiling point:
256.6±20.0 °C(Predicted)
Density 
1.156±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
0.41±0.10(Predicted)
color 
White
InChI
InChI=1S/C8H9NO3/c1-11-7-5-3-4-6(9-7)8(10)12-2/h3-5H,1-2H3
InChIKey
QCCJUEURAZMEGY-UHFFFAOYSA-N
SMILES
C1(C(OC)=O)=NC(OC)=CC=C1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41
Safety Statements 
26-39
WGK Germany 
3
HS Code 
2933399990
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6-METHOXY-PYRIDINE-2-CARBOXYLICACIDMETHYLESTER Usage And Synthesis

Uses

Methyl 6-methoxy-2-pyridinecarboxylate is a useful research chemical.

Synthesis Reference(s)

Tetrahedron Letters, 15, p. 4339, 1974 DOI: 10.1016/S0040-4039(01)92158-6

Synthesis

19621-92-2

74-88-4

26256-72-4

General procedure for the synthesis of methyl 6-methoxypyridine-2-carboxylate from 6-hydroxypyridine-2-carboxylic acid and iodomethane: 6-hydroxypyridine-2-carboxylic acid (1 g, 7.19 mmol) and silver carbonate (2.2 g, 7.90 mmol) were placed in a round-bottomed flask, and chloroform (20 mL) was added to dissolve. Subsequently, iodomethane (1 mL, 15.81 mmol) was added slowly and dropwise. The reaction mixture was stirred at 60°C for 26 hours. After completion of the reaction, the mixture was filtered and extracted with chloroform. Next, the extract was vacuum filtered and vacuum distilled to remove the solvent. Finally, the residue was purified by column chromatography (eluent ratio of ethyl acetate: hexane = 1:5) to afford the target product methyl 6-methoxypyridine-2-carboxylate (1.25 g, 100% yield).

References

[1] Patent: WO2014/3483, 2014, A1. Location in patent: Page/Page column 34
[2] Organic and Biomolecular Chemistry, 2006, vol. 4, # 6, p. 1071 - 1084
[3] Organic Letters, 2009, vol. 11, # 23, p. 5562 - 5565
[4] Patent: WO2011/79076, 2011, A1. Location in patent: Page/Page column 93

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